3ZNV
Crystal structure of the OTU domain of OTULIN at 1.3 Angstroms.
3ZNV の概要
| エントリーDOI | 10.2210/pdb3znv/pdb |
| 関連するPDBエントリー | 3ZNX |
| 分子名称 | PROTEIN FAM105B, GLYCEROL, CALCIUM ION, ... (5 entities in total) |
| 機能のキーワード | hydrolase |
| 由来する生物種 | HOMO SAPIENS (HUMAN) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 32370.56 |
| 構造登録者 | Keusekotten, K.,Elliott, P.R.,Glockner, L.,Kulathu, Y.,Wauer, T.,Krappmann, D.,Hofmann, K.,Komander, D. (登録日: 2013-02-18, 公開日: 2013-06-26, 最終更新日: 2024-05-08) |
| 主引用文献 | Keusekotten, K.,Elliott, P.R.,Glockner, L.,Fiil, B.K.,Damgaard, R.B.,Kulathu, Y.,Wauer, T.,Hospenthal, M.K.,Gyrd-Hansen, M.,Krappmann, D.,Hofmann, K.,Komander, D. Otulin Antagonizes Lubac Signaling by Specifically Hydrolyzing met1-Linked Polyubiquitin. Cell(Cambridge,Mass.), 153:1312-, 2013 Cited by PubMed Abstract: The linear ubiquitin (Ub) chain assembly complex (LUBAC) is an E3 ligase that specifically assembles Met1-linked (also known as linear) Ub chains that regulate nuclear factor κB (NF-κB) signaling. Deubiquitinases (DUBs) are key regulators of Ub signaling, but a dedicated DUB for Met1 linkages has not been identified. Here, we reveal a previously unannotated human DUB, OTULIN (also known as FAM105B), which is exquisitely specific for Met1 linkages. Crystal structures of the OTULIN catalytic domain in complex with diubiquitin reveal Met1-specific Ub-binding sites and a mechanism of substrate-assisted catalysis in which the proximal Ub activates the catalytic triad of the protease. Mutation of Ub Glu16 inhibits OTULIN activity by reducing kcat 240-fold. OTULIN overexpression or knockdown affects NF-κB responses to LUBAC, TNFα, and poly(I:C) and sensitizes cells to TNFα-induced cell death. We show that OTULIN binds LUBAC and that overexpression of OTULIN prevents TNFα-induced NEMO association with ubiquitinated RIPK1. Our data suggest that OTULIN regulates Met1-polyUb signaling. PubMed: 23746843DOI: 10.1016/J.CELL.2013.05.014 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.3 Å) |
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